EP0767826A1 - Fabric softening composition containing pentaerythritol - Google Patents

Fabric softening composition containing pentaerythritol

Info

Publication number
EP0767826A1
EP0767826A1 EP95922267A EP95922267A EP0767826A1 EP 0767826 A1 EP0767826 A1 EP 0767826A1 EP 95922267 A EP95922267 A EP 95922267A EP 95922267 A EP95922267 A EP 95922267A EP 0767826 A1 EP0767826 A1 EP 0767826A1
Authority
EP
European Patent Office
Prior art keywords
pentaerythritol
fabric softening
fabric
emulsion according
ester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP95922267A
Other languages
German (de)
French (fr)
Other versions
EP0767826B1 (en
Inventor
Andre Crutzen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Colgate Palmolive Co
Original Assignee
Colgate Palmolive Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of EP0767826A1 publication Critical patent/EP0767826A1/en
Application granted granted Critical
Publication of EP0767826B1 publication Critical patent/EP0767826B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/123Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • This invention relates to fabric softening compositions for applications to washed laundry during rinsing and/or drying cycles, to apply to the fibers of the fabrics of such laundry fabric softening amounts of fabric softening components of the compositions. More particularly, it relates to such compositions that include as fabric softening components higher fatty acid esters of pentaerythritol, of pentaerythritol oligomers, or of ethoxylated derivatives thereof, and which do not contain positively charged (i.e., cationic) emulsifiers or softeners (e.g., quaternary ammonium salts.)
  • Fabric softening compositions have long been employed to make washed laundry items softer to the touch and more comfortable to the wearer. Such compositions include solutions, emulsions, and particulate and powder products.
  • the fabric softeners of choice for most commercial products have usually been quaternary ammonium salts, such as dimethyl ditallowyl ammonium chloride, and emulsions of such softener have been added to the rinse water in the washing machine to effectively soften laundry.
  • emulsions or powder products including such fabric softener can be added to the wash water, with a detergent composition or the detergent composition can include a fabric softening component to make a so-called "softergent”.
  • R, R', R" and R"' are all alkyl groups, with at least one of such alkyls being a higher alkyl and with the others being lower alkyl(s) of 1 or 2 carbon atoms, and with X" being a salt-forming anion.
  • quaternary ammonium salt is a di-lower alkyl, di-higher alkyl ammonium halide but mono- lower alkyl tri-higher alkyl ammonium halides have also found use in some instances.
  • U.S. Patent No. 3,928,212 describes various softening agents which are polyhydric alcohol esters, but none of them is a pentaerythritol ester or an ester of an oligomer or ethoxylated derivative of pentaerythritol.
  • U.S. Patent No. 4,126,562 mentions erythritol and pentaerythritol in a list of alcohols which may be reacted with higher fatty acids to produce fabric conditioning agents, but no such compound is actually described and none is shown in a fabric softening composition or article. Also, U.S. Patent No. 4,126,562 discloses a combination of a quaternary ammonium salt fabric softener and a nonionic ester of an alcohol with a higher fatty acid, and no teaching therein that the ester would be useful alone as a fabric softener.
  • U.S. Patent No. 4,142,978 describes sorbitan esters with phase modifying components such as alkyl sulfates on a dryer sheet for softening laundry while it is being tumble-dried in an automatic laundry dryer. There is no mention in this patent of any pentaerythritol esters.
  • U.S. Patent No. 4,162,984 relates to a textile treatment emulsion of a water-insoluble cationic fabric softener which is preferably a fatty acid ester of a mono- or polyhydric alcohol or an anhydride thereof and an aromatic mono- or dicarboxylic acid.
  • a water-insoluble cationic fabric softener which is preferably a fatty acid ester of a mono- or polyhydric alcohol or an anhydride thereof and an aromatic mono- or dicarboxylic acid.
  • polyhydric alcohols that may be esterified, according to the patent, is pentaerythritol, but no pentaerythritol ester is described' specifically, nor is any oligomer of pentaerythritol suggested and none is shown to be a useful fabric softening agent in the absence of quaternary ammonium salt and aromatic carboxylic acid.
  • U.S. Patent No. 4,214,038 relates to polyglycerol esters as softening agents suitable for deposition on drying laundry from paper substrates charged to the laundry dryer with the laundry being dried.
  • polyglycerol is a polyhydric alcohol, as is pentaerythritol, it is not the same as pentaerythritol, and the patent does not suggest the use of pentaerythritol esters as fabric softeners.
  • U.S. Patent No. 5,126,060 describes a fabric softening composition based on the use of pentaerythritol esters as fabric softeners, which composition is essentially free of quat softeners. Anionic compositions, however, are not disclosed or exemplified.
  • esters of various alcohols and polyols including pentaerythritol.
  • no specific ester is described or even named and no softening composition which does not contain a quaternary ammonium compound as the fabric softener is disclosed.
  • Japanese Patent No. 90/47370 discloses fabric softening compositions based on quaternary ammonium salts which may contain higher fatty acid esters of pentaerythritol. No specific such ester is described in the abstract.
  • the present invention provides a biodegradable fabric softening aqueous emulsion which comprises from about 1 to about 25 weight percent of a pentaerythritol fabric softener, from about 0.2 to about 10 weight percent of an anionic emulsifying agent selected from the group consisting of diisotridecyl sulfosuccinate (preferred), diisodecyl sulfosuccinate and the alkali metal salt of a fatty acid, from about 0 to about 10 weight percent of a nonionic ethoxylated alcohol, and from about 65 to about 99 weight percent of aqueous medium, wherein said emulsion is essentially free of quaternary ammonium fabric softener.
  • an anionic emulsifying agent selected from the group consisting of diisotridecyl sulfosuccinate (preferred), diisodecyl sulfosuccinate and the alkali metal salt of a fatty acid,
  • the main component of the compositions of the present invention which is essentially the only fabric softening compound in such products, other than bentonite, which may also be present in them, is preferably a higher fatty acid ester of a pentaerythritol compound, which term is used in this specification to describe higher fatty acid esters of pentaerythritol, higher fatty acid esters of pentaerythritol oligomers, higher fatty acid esters of lower alkylene oxide derivatives of pentaerythritol and higher fatty acid esters of lower alkylene oxide derivatives of pentaerythritol oligomers.
  • Pentaerythritol compound may be abbreviated as PEC herein, which description and abbreviation may apply to any or all of pentaerythritol, oligomers thereof and alkyoxylated derivatives thereof, as such or as the esters, as will be indicated by the context.
  • the oligomers of pentaerythritol are preferably those of two to five pentaerythritol moieties, more preferably 2 or 3, with such moieties being joined together through single etheric bonds.
  • the lower alkylene oxide derivatives thereof are preferably of ethylene oxide or propylene oxide monomers, dimers or polymers, which terminate in hydroxyls and are joined to the pentaerythritol or oligomer of pentaerythritol through etheric linkages.
  • At least one of the PEC OH groups and preferably at least two thereof will be esterified by a higher fatty acid or other higher aliphatic acid, which can be of an odd number of carbon atoms.
  • the higher fatty acid esters of the pentaerythritol compounds are preferably partial esters and more preferably there will be at least two free hydroxyls thereon after esterification (on the pentaerythritol, oligomer or alkoxyalkane).
  • the number of such free hydroxyls is two or about two but sometimes it may be one, as in pentaerythritol tristearate, or as many as eight, as in pentaerythritol tetrapalmitate.
  • the higher aliphatic or fatty acids that may be employed as esterifying acids are those of carbon atom contents in the range of 8 to 24, preferably 12 to 22 and more preferably 12 to 18, e.g., lauric, myristic, palmitic, oleic, stearic and behenic acids. Such may be mixtures of such fatty acids, obtained from natural sources, such as coco fatty acid, commercial stearic acid, tallow acid or hydrogenated tallow acid. Of the pure fatty acids lauric and stearic acids are often preferred, sometimes depending on the pentaerythritol moiety esterified. Intermediate synthetic acids of odd numbers of carbon atoms may also be employed.
  • R1 CH 3 -- (CH 2 ) ⁇ o -- COO-
  • R 2 CH 3 -- (CH 2 ) 10 --COO--
  • R 3 OH
  • R 4 OH
  • R 1 CH 3 -- (CH 2 ) ⁇ o -- CO
  • R 2 CH 3 -- (CH 2 ) ⁇ o -- CO
  • R 3 CH 3 -- (CH 2 ) ⁇ o -- CO
  • R 4 CH 3 -- (CH 2 ) ⁇ o - CO
  • R 3 CH 3 - (CH 2 )i6 -- CO
  • R 4 CH 3 -- (CH 2 ) ⁇ 6 - CO
  • R-i CH 3 -- (CH 2 )i6 - • COO-
  • R 2 CH 3 -- (CH 2 ) ⁇ e - COO-
  • R 1 CH 3 - (CH 2 ) 20 -- COO-
  • R 2 OH
  • R 3 OH
  • R 4 OH
  • Ri CH 3 - (CH 2 ) 20 - COO-
  • R 2 CH 3 - (CH 2 ) 20 -- COO-
  • R1 CH 3 - (CH 2 ) 2 o -- COO-
  • R 2 CH 3 - (CH 2 ) 2 o - COO-
  • pentaerythritol compounds that are useful in the practice of this invention are illustrated it will be understood that various other such pentaerythritol compounds within the description thereof herein may be employed too, including such as pentaerythritol dihydrogenated tallowate, pentaerythritol ditallowate, pentaerythritol dipalmitate, and dipentaerythritol tetratallowate.
  • pentaerythritol dihydrogenated tallowate pentaerythritol ditallowate
  • pentaerythritol dipalmitate pentaerythritol dipalmitate
  • dipentaerythritol tetratallowate dipentaerythritol tetratallowate.
  • mixtures of compounds of such class are intended to be included (commercial compounds are often mixtures).
  • emulsions (which term herein is also intended to refer to dispersions and suspensions in liquid media, as well as to microemulsions [and sometimes solutions may be present, too]) of this invention will normally be aqueous emulsions in which the aqueous phase is the continuous phase, with the pentaerythritol compound being in the dispersed phase.
  • solvents and cosolvents such as ethanol, isopropanol, propylene glycol and various mono- and di-lower alkyl esters of diethylene glycol (Carbitols ®) may also be present to promote formations of stable products, when such is desirable.
  • the anionic emulsifiers which can be employed in the compositions of the present invention are diisotridecyl sulfosuccinate (preferred), diisodecyl sulfosuccinate and an alkali metal, preferably sodium, salt of a fatty acid, preferably a C 12 - C 18 fatty acid such as, for example, sodium laurate (C12), sodium myristate (C 1 ), sodium palmitate (C ⁇ 6 ) and sodium stearate (C ⁇ ).
  • the optional nonionic emulsifiers of the present invention are higher alkyl ethers which contain one or more hydroxyalkyl substituents.
  • Such ethers are known as ethoxylated alcohols and can be symbolized as, for example, C-
  • ethoxylated alcohols are those identified by the followi
  • the PEC will be employed without the presence of any other fabric softening material but it is possible to utilize such other materials with it if they are not ecologically unacceptable and if they do not interfere with the softening action of the PEC.
  • such additions may be important because although PEC's have some antistatic properties sometimes they are not sufficient for the intended purposes.
  • antistatic quats are to be avoided, not only because when they are present there can be ecological problems, due to their toxicities to aquatic organisms, but because their cationic character is contra of the anionic character of the invented compositions. It should be kept in mind, therefore, when employing supplementary fabric softeners and antistats, that they should not change the anionic nature of the composition and they should not make the composition in which they are incorporated of greater ecotoxicity than is allowed by regulatory authorities in the area of intended use.
  • compositions include the usual adjuvants that normally are present in other fabric softening compositions, such as perfumes, fixatives, solvents, cosolvents, hydrotropes, antioxidants, stabilizers, biodegradable antimicrobials, fillers, thickeners and fluorescent brighteners, all of which are known classes of materials in the fabric softening compositions field, with examples of several of these being given in the art mentioned in this specification, all of which is hereby incorporated herein by reference.
  • adjuvants that normally are present in other fabric softening compositions, such as perfumes, fixatives, solvents, cosolvents, hydrotropes, antioxidants, stabilizers, biodegradable antimicrobials, fillers, thickeners and fluorescent brighteners, all of which are known classes of materials in the fabric softening compositions field, with examples of several of these being given in the art mentioned in this specification, all of which is hereby incorporated herein by reference.
  • the last component of the present compositions which is required in the aqueous emulsions, is water.
  • any clean water can be employed, such as any of a hardness in the range of 0 to 500 p.p.m., as CaC0 3 , but it will be preferred to use water of a hardness of no more than 150 p.p.m., more preferably less than 50 p.p.m., and most preferably the water will be deionized water that has been irradiated.
  • the proportions of components of the invented compositions will be chose which result in stable and effective products for fabric softening applications.
  • the concentration by weight in such compositions will normally be in the range of about 1 to 25%, and preferably about 3 to 7%, e.g., about 5%.
  • the content of anionic emulsifier(s) will normally be in the range of about 0.2 to 10%, preferably about 1 to 3%.
  • the content of the optional nonionic ethoxylated alcohol(s) will be in the range of 0 to 10%, preferably 0 to 0.25%.
  • the aqueous medium or water content of these compositions is the balance thereof, usually being in the range of about 65 to 99%, preferably about 90 to 95%, e.g., about 93.75%. It is to be understood that the presence of any adjuvants or supplemental components of the emulsions will be compensated for by corresponding decreases in the water contents of the compositions. Usually the total adjuvants content will be nor more than 25%, preferably will be no more than 15% and in many instances will be held to a limit of 5%. None of the adjuvants employed will be such as to cause unacceptable levels of toxicity which could adversely affect aquatic organisms, including fish that inhabit lakes and streams into which there are fed washing machine rinses that had been charged with the present compositions.
  • the invented compositions is comparatively simple but to produce applicant's desired stable emulsions (and microemulsions) a particular process is desirably followed.
  • the PEC and the anionic emulsifier be mixed together and melted before addition to the aqueous medium.
  • the two meltable materials, PEC and anionic emulsifier may be separately melted and added together or simultaneously to the aqueous medium (usually water), which should also be at about the same elevated temperature, about 60°C, for example.
  • the water employed is desirably acidified, as by addition to it of HCI or other suitable acid, until the pH thereof is in the range of 2 to 7, preferably 2.5 to 5.5, e.g., about 3.5.
  • the emulsion is based on the use of a fatty acid salt as the anionic emulsifier, it is preferably generated in situ by neutralizing the corresponding fatty acid which is introduced together with the PEC.
  • the water employed desirably contains an amount of NaOH or other suitable base sufficient to neutralize the fatty acid content in the emulsion produced by the fatty acid salt.
  • the emulsion produced may be cooled to room temperature, with the nonionic ethoxylated alcohol emulsifier being added before or after such cooling, preferably before.
  • the nonionic emulsifier if not already in a liquid state, be heated to a liquid or molten state prior to its addition to the warm emulsion.
  • the result is a stable emulsion, which resists separation after a test period of three months at room temperature (about 18-25°C), although some coacervation is observed in the composition containing sodium laurate as the sole anionic emulsifier.
  • the various invented compositions are employed in the same manners as other emulsions that apply fabric softener to laundry.
  • the emulsion may be added to rinse water, with the concentrations of PEC being in the range of about 0.01 to 0.05% of the rinse water.
  • such compositions may be added to the wash water but in such cases the concentrations may be increased, often about 1 to 3 times.
  • the following examples illustrate but do not limit the invention. Unless otherwise indicated all parts and percentages in this specification and the appended claims are by weight and all temperatures are in °C.
  • a stable emulsion is made of the above formula by heating together the pentaerythritol ditallowate and the diisotridecyl sulfosuccinate to 60°C and then admixing such melted mixture with the 60°C acidified water after which the nonionic component, C 16 -C 18 Eg, also at 60°C, is admixed with the water emulsion of pentaerythritol ditallowate and diisotridecyl sulfosuccinate.
  • the resulting stable anionic emulsion which is at a pH of about 3.5, is a good fabric softening composition.
  • PEC pentaerythritol ditallowate
  • other relatively effective PEC's include pentaerythritol dilaurate, pentaerythritol distearate and pentaerythritol di-hydrogenated tallowate.
  • Diisodecyl sulfosuccinate may be utilized as the anionic component in the above formulation but with lesser fabric softening efficacy.
  • a stable emulsion is made of the above formula by heating together the pentaerythritol ditallowate and the sodium myristate to 60°C and then admixing such melted mixture with the 60°C basified water after which the nonionic component, also at 60°C, is admixed with the water emulsion of pentaerythritol ditallowate and sodium myristate.
  • the resulting anionic emulsion is not only a good fabric softening composition, but the use of a fatty acid soap such as sodium myristate, and, alternatively, sodium laurate, sodium palmitate, sodium stearate and the like, is relatively inexpensive and the soap itself imparts some softness to the composition.
  • a stable emulsion is made of each formulation by preparing a molten mixture of the first three or four components, as the case may be, which is then poured into the warmed deionized water (60°C) with stirring, to which is then added the hydrochloric acid.
  • Molten mixture of ditallowate and myristic acid are added in warm deionized water (60°C) containing NaOH to provide the indicated amount of sodium myristate: 1% myristic acid; 4.4% NaOH solution (40 g/L).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

An anionic fabric softening emulsion composition containing a pentaerythritol softener, an anionic emulsifying agent, and, optionally, a nonionic emulsifier.

Description

FABRIC SOFTENING COMPOSITION CONTAINING PENTAERYTHRITOL
Field of the Invention
This invention relates to fabric softening compositions for applications to washed laundry during rinsing and/or drying cycles, to apply to the fibers of the fabrics of such laundry fabric softening amounts of fabric softening components of the compositions. More particularly, it relates to such compositions that include as fabric softening components higher fatty acid esters of pentaerythritol, of pentaerythritol oligomers, or of ethoxylated derivatives thereof, and which do not contain positively charged (i.e., cationic) emulsifiers or softeners (e.g., quaternary ammonium salts.)
Discussion of the Prior Art
Fabric softening compositions have long been employed to make washed laundry items softer to the touch and more comfortable to the wearer. Such compositions include solutions, emulsions, and particulate and powder products. The fabric softeners of choice for most commercial products have usually been quaternary ammonium salts, such as dimethyl ditallowyl ammonium chloride, and emulsions of such softener have been added to the rinse water in the washing machine to effectively soften laundry. Alternatively, such emulsions or powder products including such fabric softener can be added to the wash water, with a detergent composition or the detergent composition can include a fabric softening component to make a so-called "softergent".
Although various fabric softening (and antistatic) compositions have been commercially marketed, with varying degrees of commercial success, over the years and although various fabric softening components thereof have been included in them the most successful of such components have been the quaternary ammonium salts. Such compounds are of the formula
wherein R, R', R" and R"' are all alkyl groups, with at least one of such alkyls being a higher alkyl and with the others being lower alkyl(s) of 1 or 2 carbon atoms, and with X" being a salt-forming anion. Preferably, such quaternary ammonium salt is a di-lower alkyl, di-higher alkyl ammonium halide but mono- lower alkyl tri-higher alkyl ammonium halides have also found use in some instances.
While such quaternary ammonium salts have been effective fabric softeners in the described applications they are characterized by disadvantageous properties too, which have led to attempts to find replacements for them. For example, being cationic, they tend to react with anionic materials, sometimes to the detriment of their intended fabric softening function. Moreover, they are not as readily biodegradable as is desirable and they have been found to be toxic to aquatic organisms, which could lead to harmful effects on aquatic life in lakes, rivers and other waters into which waste waters carrying such compounds could be emptied.
In efforts to find replacements for quaternary ammonium salts as fabric softeners, neoalkanamides, glyceryl esters, glycol esters, silicones, cationic- anionic complexes, bentonite and various lubricants have been suggested for use alone or in conjunction with reduced amounts of the quaternary ammonium salts but frequently the softening effects thereof were insufficient or the replacement softeners possessed other characteristics which made them less desirable than the quaternary ammonium salts, despite the disadvantages thereof. Now, however, applicants have discovered an anionic composition that can satisfactorily soften laundry and that does not exhibit the adverse effects of the quaternary ammonium salts on aquatic organisms. This is an especially important discovery at this time when the seriousness of the problem is being recognized and when several countries are passing laws and promulgating regulations prohibiting the incorporation of some quaternary ammonium compounds in products that may be discharged into sewage and drainage systems and, ultimately, into bodies of water wherein the possibility of toxic effects on aquatic life exists.
In application Serial No. 07/755,965 filed September 6, 1991; Serial No. 07/756,030 filed September 6, 1991; Serial No. 07/638,945 filed January 9, 1991; and Serial No. 07/945,715 filed September 16, 1992; the entire contents and disclosures of each of which are incorporated herein by reference, there are described certain higher fatty acid esters of pentaerythritol, pentaerythritol oligomers and ethoxylated derivatives thereof which function as fabric softeners in conjunction with dispersing agents therefor.
U.S. Patent No. 3,928,212 describes various softening agents which are polyhydric alcohol esters, but none of them is a pentaerythritol ester or an ester of an oligomer or ethoxylated derivative of pentaerythritol.
U.S. Patent No. 4,126,562 mentions erythritol and pentaerythritol in a list of alcohols which may be reacted with higher fatty acids to produce fabric conditioning agents, but no such compound is actually described and none is shown in a fabric softening composition or article. Also, U.S. Patent No. 4,126,562 discloses a combination of a quaternary ammonium salt fabric softener and a nonionic ester of an alcohol with a higher fatty acid, and no teaching therein that the ester would be useful alone as a fabric softener.
U.S. Patent No. 4,142,978 describes sorbitan esters with phase modifying components such as alkyl sulfates on a dryer sheet for softening laundry while it is being tumble-dried in an automatic laundry dryer. There is no mention in this patent of any pentaerythritol esters.
U.S. Patent No. 4,162,984 relates to a textile treatment emulsion of a water-insoluble cationic fabric softener which is preferably a fatty acid ester of a mono- or polyhydric alcohol or an anhydride thereof and an aromatic mono- or dicarboxylic acid. Among the polyhydric alcohols that may be esterified, according to the patent, is pentaerythritol, but no pentaerythritol ester is described' specifically, nor is any oligomer of pentaerythritol suggested and none is shown to be a useful fabric softening agent in the absence of quaternary ammonium salt and aromatic carboxylic acid. Although the patentees were aware of the disadvantages of the quaternary ammonium salt component (reaction with anionic detergent from the wash cycle) and found that its content could be reduced if the pentaerythritol ester and aromatic carboxylic acid were present, they never recognized and apparently never made a fabric softening composition which did not contain quaternary ammonium halide or equivalent cationic fabric softener.
U.S. Patent No. 4,214,038 relates to polyglycerol esters as softening agents suitable for deposition on drying laundry from paper substrates charged to the laundry dryer with the laundry being dried. Although polyglycerol is a polyhydric alcohol, as is pentaerythritol, it is not the same as pentaerythritol, and the patent does not suggest the use of pentaerythritol esters as fabric softeners. U.S. Patent No. 5,126,060 describes a fabric softening composition based on the use of pentaerythritol esters as fabric softeners, which composition is essentially free of quat softeners. Anionic compositions, however, are not disclosed or exemplified. Although cationic and nonionic emulsifiers are disclosed, such as ethoxylated amines and ethoxylated alcohols, the use of applicant's specified anionic emulsifiers is neither disclosed nor exemplified. European Patent Specification No. 276999-A mentions fabric conditioning compositions containing a non-cationic fabric softener and a nonionic cellulose ether. Although esters of polyhydric alcohols are mentioned as suitable conditioning agents, pentaerythritol esters are not disclosed therein. German Patent Specification No. 3612479-A describes textile softening compositions containing quaternary ammonium compounds with carboxylic esters. Among the carboxylic acid esters mentioned are esters of various alcohols and polyols, including pentaerythritol. However, no such specific ester is described or even named and no softening composition which does not contain a quaternary ammonium compound as the fabric softener is disclosed. Japanese Patent No. 90/47370 discloses fabric softening compositions based on quaternary ammonium salts which may contain higher fatty acid esters of pentaerythritol. No specific such ester is described in the abstract.
In none of the disclosures mentioned above it is taught that any pentaerythritol ester could be employed with a suitable anionic dispersing agent, optionally with a suitable nonionic emulsifier, as a fabric softener in place of a quat softener which would have advantageous softening action. Thus, none of the references, either alone or in combination with any of the others, anticipates the present invention or makes it obvious.
Brief Summary of the Invention
The present invention provides a biodegradable fabric softening aqueous emulsion which comprises from about 1 to about 25 weight percent of a pentaerythritol fabric softener, from about 0.2 to about 10 weight percent of an anionic emulsifying agent selected from the group consisting of diisotridecyl sulfosuccinate (preferred), diisodecyl sulfosuccinate and the alkali metal salt of a fatty acid, from about 0 to about 10 weight percent of a nonionic ethoxylated alcohol, and from about 65 to about 99 weight percent of aqueous medium, wherein said emulsion is essentially free of quaternary ammonium fabric softener. Detailed Description of the Invention
The main component of the compositions of the present invention, which is essentially the only fabric softening compound in such products, other than bentonite, which may also be present in them, is preferably a higher fatty acid ester of a pentaerythritol compound, which term is used in this specification to describe higher fatty acid esters of pentaerythritol, higher fatty acid esters of pentaerythritol oligomers, higher fatty acid esters of lower alkylene oxide derivatives of pentaerythritol and higher fatty acid esters of lower alkylene oxide derivatives of pentaerythritol oligomers. Pentaerythritol compound may be abbreviated as PEC herein, which description and abbreviation may apply to any or all of pentaerythritol, oligomers thereof and alkyoxylated derivatives thereof, as such or as the esters, as will be indicated by the context.
The oligomers of pentaerythritol are preferably those of two to five pentaerythritol moieties, more preferably 2 or 3, with such moieties being joined together through single etheric bonds. The lower alkylene oxide derivatives thereof are preferably of ethylene oxide or propylene oxide monomers, dimers or polymers, which terminate in hydroxyls and are joined to the pentaerythritol or oligomer of pentaerythritol through etheric linkages. Preferably there will be one to ten alkylene oxide moieties in each such alkylene oxide chain, more preferably 2 to 6, and there will be one to ten such groups on a PEC, depending on the oligomer. At least one of the PEC OH groups and preferably at least two thereof will be esterified by a higher fatty acid or other higher aliphatic acid, which can be of an odd number of carbon atoms. The higher fatty acid esters of the pentaerythritol compounds are preferably partial esters and more preferably there will be at least two free hydroxyls thereon after esterification (on the pentaerythritol, oligomer or alkoxyalkane). Usually the number of such free hydroxyls is two or about two but sometimes it may be one, as in pentaerythritol tristearate, or as many as eight, as in pentaerythritol tetrapalmitate.
The higher aliphatic or fatty acids that may be employed as esterifying acids are those of carbon atom contents in the range of 8 to 24, preferably 12 to 22 and more preferably 12 to 18, e.g., lauric, myristic, palmitic, oleic, stearic and behenic acids. Such may be mixtures of such fatty acids, obtained from natural sources, such as coco fatty acid, commercial stearic acid, tallow acid or hydrogenated tallow acid. Of the pure fatty acids lauric and stearic acids are often preferred, sometimes depending on the pentaerythritol moiety esterified. Intermediate synthetic acids of odd numbers of carbon atoms may also be employed.
Examples of some esters within the present invention follow: MONOPENTAERYTHRITOL ESTERS
CH2 — R2
I R*ι — CH2 — C ~ CH2 -- R3
I CH2 -- R4
MONOPENTAERYTHRITOL DILAURATE
R1 = CH3 -- (CH2)ιo -- COO- R2 = CH3 -- (CH2)10--COO-- R3 = OH R4 = OH
MONOPENTAERYTHRITOL MONSTEARATE
R1 = CH3 -- (CH2)i6 -- COO-- R2 = OH
R3 = OH R4 = OH
DIPENTAERYTHRITOL ESTERS CH20R! CH2OR2
I I
HO CH2 -- C -- CH2 - 0 -- CH2 -- C -- CH2OH I I
CH2OR3 CH2OR4
DIPENTAERYTHRITOL TETRALAURATE
R1 = CH3 -- (CH2)ιo -- CO R2 = CH3 -- (CH2)ιo -- CO
R3 = CH3 -- (CH2)ιo -- CO R4 = CH3 -- (CH2)ιo - CO
DIPENTAERYTHRITOL TETRASTEARATE R1 = CH3 - (CH26 -- CO R2 = CH3 - (CH^ 6 -- CO
R3 = CH3 - (CH2)i6 -- CO R4 = CH3 -- (CH26 - CO
MONOPENTAERYTHRITOL DISTEARATE
R-i = CH3 -- (CH2)i6 - COO- R2 = CH3 -- (CH2)ιe - COO-
R3 = OH R4 = OH MONOPENTAERYTHRITOL TRISTEARATE
RT = CH3 - (CH2)i6 -- COO- R2 = CH3 - (CH26 - COO-
R3 = CH3 - (CH2)*ι 6 " COO- R4 = OH
MONOPENTAERYTHRITOL MONBEHENATE
R1 = CH3 - (CH2)20 -- COO- R2 = OH R3 = OH R4 = OH
MONOPENTAERYTHRITOL DIBEHENATE
Ri = CH3 - (CH2)20 - COO- R2 = CH3 - (CH2)20 -- COO-
R3 = OH R4 = OH
PENTAERYTHRITOL 10 ETHYLENE OXIDE ESTER
CH2 » O -- CH2 - CH20)nH I
R1 — CH — C — • CH2 — * R2 I CH2 - O - CH2 - CH20)n' H with n -r- n' = 10
MONOPENTAERYTHRITOL 10 ETHYLENE OXIDE DISTEARATE R1 = CH3 - (CH26 -- COO- R2 = CH3 - (CH26 -- COO- PENTAERYTHRITOL 4 PROPYLENE OXIDE ESTERS
CH2 -- O - CH2 -- CH - CH20)2H
I RT- CH2 -- C -- CH2 -- R2
I CH2 -- O - CH2 -- CH - CH20)2H
MONOPENTAERYTHRITOL
4 PROPYLENE OXIDE MONSTEARATE
R1 = CH3 - (C 2 6 " COO- R2 = OH
MONOPENTAERYTHRITOL
4 PROPYLENE OXIDE DISTEARATE R1 = CH3 -- (CH2)i6 -- COO- R2 = CH3 - (CH26 -- COO-
MONOPENTAERYTHRITOL
4 PROPYLENE OXIDE MONOBEHENATE
RT = CH3 » (CH2)20 -- COO- R2 = OH
MONOPENTAERYTHRITOL 4 PROPYLENE OXIDE DIBEHENATE
R1 = CH3 - (CH2)2o -- COO- R2 = CH3 - (CH2)2o - COO-
Although in the formulas given herein some preferred pentaerythritol compounds that are useful in the practice of this invention are illustrated it will be understood that various other such pentaerythritol compounds within the description thereof herein may be employed too, including such as pentaerythritol dihydrogenated tallowate, pentaerythritol ditallowate, pentaerythritol dipalmitate, and dipentaerythritol tetratallowate. Also, in this specification when reference is to a compound of a class, unless it is indicated otherwise therein it is to be considered that the employment of mixtures of compounds of such class are intended to be included (commercial compounds are often mixtures).
The emulsions (which term herein is also intended to refer to dispersions and suspensions in liquid media, as well as to microemulsions [and sometimes solutions may be present, too]) of this invention will normally be aqueous emulsions in which the aqueous phase is the continuous phase, with the pentaerythritol compound being in the dispersed phase. However, solvents and cosolvents, such as ethanol, isopropanol, propylene glycol and various mono- and di-lower alkyl esters of diethylene glycol (Carbitols ®) may also be present to promote formations of stable products, when such is desirable. The anionic emulsifiers which can be employed in the compositions of the present invention are diisotridecyl sulfosuccinate (preferred), diisodecyl sulfosuccinate and an alkali metal, preferably sodium, salt of a fatty acid, preferably a C12 - C18 fatty acid such as, for example, sodium laurate (C12), sodium myristate (C1 ), sodium palmitate (Cι6) and sodium stearate (Cιβ). The optional nonionic emulsifiers of the present invention are higher alkyl ethers which contain one or more hydroxyalkyl substituents. Of these the more preferred are the higher alkyl lower di- or polyethylene glycol ethers of 2.5 to 12 ethoxy groups (4 to 24 carbon atoms), preferably the higher alkyl diethylene glycol ethers, in which the higher alkyl is of 8 to 24, preferably 12 to 18 carbon atoms. Such ethers are known as ethoxylated alcohols and can be symbolized as, for example, C-|4 - C15 Eg wherein C with is numerical subscript represents the average carbon atom content of the alcohol function and E with its numerical subscript represents the number of ethoxy functions in the resultant ether. Among the preferred ethoxylated alcohols are those identified by the followi
The foregoing ethoxylated alcohols are supplied under the tradename
"Dobanol" by Shell Chemicals (Amsterdam -The Netherlands); under the tradename "Synperonic" by ICI Surfactants (Cleveland-U.K.); and by Condea Chemie (Brunsbuettel-Germany).
Normally, the PEC will be employed without the presence of any other fabric softening material but it is possible to utilize such other materials with it if they are not ecologically unacceptable and if they do not interfere with the softening action of the PEC. In fact, sometimes, when antistatic action is desirable in the product, such additions may be important because although PEC's have some antistatic properties sometimes they are not sufficient for the intended purposes. Thus, it is possible to formulate fabric softening compositions with the PEC supplemented by other fabric softeners and antistatic agents. However, for purposes of this invention, use of antistatic quats are to be avoided, not only because when they are present there can be ecological problems, due to their toxicities to aquatic organisms, but because their cationic character is contra of the anionic character of the invented compositions. It should be kept in mind, therefore, when employing supplementary fabric softeners and antistats, that they should not change the anionic nature of the composition and they should not make the composition in which they are incorporated of greater ecotoxicity than is allowed by regulatory authorities in the area of intended use.
Other materials that may be incorporated in the invented compositions include the usual adjuvants that normally are present in other fabric softening compositions, such as perfumes, fixatives, solvents, cosolvents, hydrotropes, antioxidants, stabilizers, biodegradable antimicrobials, fillers, thickeners and fluorescent brighteners, all of which are known classes of materials in the fabric softening compositions field, with examples of several of these being given in the art mentioned in this specification, all of which is hereby incorporated herein by reference.
The last component of the present compositions, which is required in the aqueous emulsions, is water. Normally, any clean water can be employed, such as any of a hardness in the range of 0 to 500 p.p.m., as CaC03, but it will be preferred to use water of a hardness of no more than 150 p.p.m., more preferably less than 50 p.p.m., and most preferably the water will be deionized water that has been irradiated. The proportions of components of the invented compositions will be chose which result in stable and effective products for fabric softening applications. For the PEC's the concentration by weight in such compositions will normally be in the range of about 1 to 25%, and preferably about 3 to 7%, e.g., about 5%. For the emulsions the content of anionic emulsifier(s) will normally be in the range of about 0.2 to 10%, preferably about 1 to 3%. The content of the optional nonionic ethoxylated alcohol(s) will be in the range of 0 to 10%, preferably 0 to 0.25%.
The aqueous medium or water content of these compositions is the balance thereof, usually being in the range of about 65 to 99%, preferably about 90 to 95%, e.g., about 93.75%. It is to be understood that the presence of any adjuvants or supplemental components of the emulsions will be compensated for by corresponding decreases in the water contents of the compositions. Usually the total adjuvants content will be nor more than 25%, preferably will be no more than 15% and in many instances will be held to a limit of 5%. None of the adjuvants employed will be such as to cause unacceptable levels of toxicity which could adversely affect aquatic organisms, including fish that inhabit lakes and streams into which there are fed washing machine rinses that had been charged with the present compositions.
To manufacture the invented compositions is comparatively simple but to produce applicant's desired stable emulsions (and microemulsions) a particular process is desirably followed. To produce the desired stable emulsions it is preferable that the PEC and the anionic emulsifier be mixed together and melted before addition to the aqueous medium. Alternatively, the two meltable materials, PEC and anionic emulsifier, may be separately melted and added together or simultaneously to the aqueous medium (usually water), which should also be at about the same elevated temperature, about 60°C, for example. When the emulsion is based on the use of diisotridecyl sulfosuccinate as the anionic emulsifier, the water employed is desirably acidified, as by addition to it of HCI or other suitable acid, until the pH thereof is in the range of 2 to 7, preferably 2.5 to 5.5, e.g., about 3.5.
When the emulsion is based on the use of a fatty acid salt as the anionic emulsifier, it is preferably generated in situ by neutralizing the corresponding fatty acid which is introduced together with the PEC. The water employed desirably contains an amount of NaOH or other suitable base sufficient to neutralize the fatty acid content in the emulsion produced by the fatty acid salt. After the mixing, the emulsion produced may be cooled to room temperature, with the nonionic ethoxylated alcohol emulsifier being added before or after such cooling, preferably before. For purposes of homogeneity, it is preferred that the nonionic emulsifier, if not already in a liquid state, be heated to a liquid or molten state prior to its addition to the warm emulsion. The result is a stable emulsion, which resists separation after a test period of three months at room temperature (about 18-25°C), although some coacervation is observed in the composition containing sodium laurate as the sole anionic emulsifier.
In use, the various invented compositions are employed in the same manners as other emulsions that apply fabric softener to laundry. The emulsion may be added to rinse water, with the concentrations of PEC being in the range of about 0.01 to 0.05% of the rinse water. Alternatively, such compositions may be added to the wash water but in such cases the concentrations may be increased, often about 1 to 3 times. The following examples illustrate but do not limit the invention. Unless otherwise indicated all parts and percentages in this specification and the appended claims are by weight and all temperatures are in °C.
EXAMPLE 1 I
Component Weiαht Percent
Pentaerythritol ditallowate 4.9
Diisotridecyl sulfosuccinate 1.0
Cl6 " Ci8 Eg 0.25
Hydrochloric acid (concentrated) 0.1
Water, deionized, q.s. ad 100%
A stable emulsion is made of the above formula by heating together the pentaerythritol ditallowate and the diisotridecyl sulfosuccinate to 60°C and then admixing such melted mixture with the 60°C acidified water after which the nonionic component, C16-C18 Eg, also at 60°C, is admixed with the water emulsion of pentaerythritol ditallowate and diisotridecyl sulfosuccinate. The resulting stable anionic emulsion, which is at a pH of about 3.5, is a good fabric softening composition. In a variation of the formula of this Example, instead of pentaerythritol ditallowate, other relatively effective PEC's include pentaerythritol dilaurate, pentaerythritol distearate and pentaerythritol di-hydrogenated tallowate.
Diisodecyl sulfosuccinate may be utilized as the anionic component in the above formulation but with lesser fabric softening efficacy.
EXAMPLE 2
Component Weight Percent
Pentaerythritol ditallowate 5.2
Sodium myristate 1.1
Ci6 - C18 E5 + C16 - Ci8 E7. ratio 1:1.6 1.4
Sodium hydroxide 1M 4.3 Water, deionized, q.s. ad 100%
A stable emulsion is made of the above formula by heating together the pentaerythritol ditallowate and the sodium myristate to 60°C and then admixing such melted mixture with the 60°C basified water after which the nonionic component, also at 60°C, is admixed with the water emulsion of pentaerythritol ditallowate and sodium myristate. The resulting anionic emulsion is not only a good fabric softening composition, but the use of a fatty acid soap such as sodium myristate, and, alternatively, sodium laurate, sodium palmitate, sodium stearate and the like, is relatively inexpensive and the soap itself imparts some softness to the composition.
The invention has been described with respect to various working examples and embodiments thereof but it is not to be considered to be limited to those because one of skill-in-the-art, with the present specification before him or her, will be able to utilized substitutes and equivalents without departing from the invention.
EXAMPLE 3
Component Weiαht Percent
A B C
Pentaerythritol ditallowate 4.9 4.9 4.9 Diisotridecyl sulfosuccinate 1.0 1.0 0.0
C-|3 - C-I5 Eg 0.0 0.25 0.25
Odorant 0.32 0.32 0.32 Hydrochloric acid (cone.) 0.1 0.1 0.1
Deionized water, q.s. ad 100%
A stable emulsion is made of each formulation by preparing a molten mixture of the first three or four components, as the case may be, which is then poured into the warmed deionized water (60°C) with stirring, to which is then added the hydrochloric acid.
Experimental results observed on the fabric softening efficacy of each emulsion formulation on similarly treated fabrics indicates that removal of the nonionic component from the composition (A versus B) significantly improves its softening performance. Conversely, in the presence of the nonionic, the softening performance is not significantly modified by the removal of the anionic component (B versus C).
Experimental conditions: lab minisoftening machine with desized terry towels; 4.4 g/L in tap water; swatches dried and conditioned at 21 °C, 50% RH; pair comparison.
EXAMPLE 4
Component Weiαht Percent
B
Pentaerythritol ditallowate 5.2 5.2 5.2 Sodium myristate * 1.1 1.1 0.0 C16-C18 E5 + C16-Ci8 E7, ratio 1:1.6 0.0 1.4 1.4 Deionized water, q.s. ad 100%
Molten mixture of ditallowate and myristic acid are added in warm deionized water (60°C) containing NaOH to provide the indicated amount of sodium myristate: 1% myristic acid; 4.4% NaOH solution (40 g/L).
A stable emulsion of each of the above formulations is made and then experimentally tested for fabric softening efficacy as in Example 3 with similar results.

Claims

What is claimed is:
1. A fabric softening aqueous emulsion which comprises by weight from about 1 to about 25% of a higher aliphatic acid ester of pentaerythritol, of an oligomer of pentaerythritol, of a lower alkylene oxide derivative of pentaerythritol or of a lower alkylene oxide derivative of an oligomer of pentaerythritol, or a mixture of any two or more thereof, from about 0.2 to about 10% of an anionic emulsifying agent selected from the group consisting of diisotridecyl sulfosuccinate, diisodecyl sulfosuccinate, and the alkali metal salt of a fatty acid, from about 0 to about 10% of an ethoxylated alcohol emulsifier, and from about 65 to about 99% of aqueous medium, wherein said emulsion is essentially free of cationic emulsifiers and fabric softeners.
2. A fabric softening emulsion according to claim 1 wherein said pentaerythritol ester is pentaerythritol ditallowate, pentaerythritol dilaurate, pentaerythritol distearate or pentaerythritol di-hydrogenated tallowate.
3. A fabric softening emulsion according to claim 1 wherein said pentaerythritol ester is pentaerythritol ditallowate.
4. A fabric softening emulsion according to claim 1 wherein said anionic emulsifying agent is diisotridecyl sulfosuccinate or sodium myristate.
5. A fabric softening emulsion according to claim 1 wherein said pentaerythritol ester is pentaerythritol ditallowate and said anionic emulsifying agent is diisotridecyl sulfosuccinate or sodium myristate.
6. A fabric softening emulsion according to claim 1 wherein the amount of said pentaerythritol ester is from about 3 to about 7 percent.
7. A fabric softening emulsion according to claim 1 where the amount of said anionic emulsifying agent is from about 1 to about 3%.
8. A fabric softening emulsion according to claim 1 where the amount of said ethoxylated alcohol emulsifier is from about 0 to 0.25%.
EP95922267A 1994-06-13 1995-06-08 Fabric softening composition containing pentaerythritol Expired - Lifetime EP0767826B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US258297 1994-06-13
US08/258,297 US5419842A (en) 1994-06-13 1994-06-13 Anionic fabric softening composition containing pentaerythritol softener
PCT/US1995/007317 WO1995034622A1 (en) 1994-06-13 1995-06-08 Fabric softening composition containing pentaerythritol

Publications (2)

Publication Number Publication Date
EP0767826A1 true EP0767826A1 (en) 1997-04-16
EP0767826B1 EP0767826B1 (en) 2001-10-10

Family

ID=22979967

Family Applications (1)

Application Number Title Priority Date Filing Date
EP95922267A Expired - Lifetime EP0767826B1 (en) 1994-06-13 1995-06-08 Fabric softening composition containing pentaerythritol

Country Status (9)

Country Link
US (1) US5419842A (en)
EP (1) EP0767826B1 (en)
AT (1) ATE206747T1 (en)
AU (1) AU2701095A (en)
DE (1) DE69523158T2 (en)
DK (1) DK0767826T3 (en)
ES (1) ES2165423T3 (en)
PT (1) PT767826E (en)
WO (1) WO1995034622A1 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2192800C (en) * 1994-07-26 2000-12-05 Mark Robert Sivik Rinse added fabric softener compositions containing antioxidants for sun-fade protection for fabrics
EP0879277B1 (en) * 1996-01-19 2001-10-17 Unilever Plc Non-cationic systems for dryer sheets
DE19732073C1 (en) * 1997-07-25 1998-08-20 Henkel Kgaa Storage-stable liquid nitrogen-free textile softener in non-microemulsion form
GB9911437D0 (en) * 1999-05-17 1999-07-14 Unilever Plc Fabric softening compositions
EP1396536B1 (en) * 2002-09-05 2005-10-19 The Procter & Gamble Company Structuring systems for fabric treatment compostions
US7371718B2 (en) * 2005-04-22 2008-05-13 The Dial Corporation Liquid fabric softener
WO2012098177A1 (en) * 2011-01-21 2012-07-26 Basf Se Use of tallow alcohol ethoxylates in machine dish washing
CN114746603A (en) 2019-12-20 2022-07-12 花王株式会社 Softening base
CA3196789A1 (en) 2020-12-23 2022-06-30 Ashish Dhawan Non-cationic softeners and methods of use

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL249601A (en) * 1959-03-21
GB1257928A (en) * 1968-11-28 1971-12-22
JPS5130638B2 (en) * 1972-07-12 1976-09-02
AU510901B2 (en) * 1976-01-09 1980-07-17 Procter & Gamble Company, The Fabric softening method and device
JPH0247362A (en) * 1988-08-03 1990-02-16 Kao Corp Soft-finishing agent
US5015414A (en) * 1988-09-08 1991-05-14 Kao Corporation Low-irritant detergent composition containing alkyl saccharide and sulfosuccinate surfactants
GB8824600D0 (en) * 1988-10-20 1988-11-23 Unilever Plc Detergent composition
US5332513A (en) * 1990-01-09 1994-07-26 Colgate-Palmolive Co. Particulate fabric softening and detergent compositions
US5126060A (en) * 1991-01-09 1992-06-30 Colgate-Palmolive Co. Biodegradable fabric softening compositions based on pentaerythritol esters and free of quaternary ammonium compounds
ZA936280B (en) * 1992-09-16 1995-05-26 Colgate Palmolive Co Fabric softening composition based on higher fatty acid ester and dispersant for such ester

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9534622A1 *

Also Published As

Publication number Publication date
AU2701095A (en) 1996-01-05
US5419842A (en) 1995-05-30
DE69523158D1 (en) 2001-11-15
EP0767826B1 (en) 2001-10-10
DE69523158T2 (en) 2002-07-11
DK0767826T3 (en) 2002-02-04
ATE206747T1 (en) 2001-10-15
WO1995034622A1 (en) 1995-12-21
PT767826E (en) 2002-03-28
ES2165423T3 (en) 2002-03-16

Similar Documents

Publication Publication Date Title
US5290459A (en) Biodegradable fabric softening compositions based on pentaerythritol esters and free of quaternary ammonium compounds
US5358647A (en) Fabric softening products based on a combination of pentaerythritol compound and bentonite
CA2243955C (en) Fabric care compositions including dispersible polyolefin and method for using same
EP0530958B1 (en) Fabric softening products based on a combination of pentaerythritol compound and montmorillonite
JPH05106166A (en) Fiber product softened composition and manufacture of said composition
JPH0610266A (en) Rinse conditioner
US5419842A (en) Anionic fabric softening composition containing pentaerythritol softener
US5593614A (en) Fabric softening composition based on higher fatty acid ester and dispersant for such ester
EP0530959B1 (en) Fabric softening compositions based on pentaerythritol compound and dispersant for such a compound
CA1329682C (en) Isotropic fabric softener composition containing fabric mildewstat
KR900009221B1 (en) Method of conditioning fabrics
JPH03113074A (en) Composition for softening liquid textile product
JP3274940B2 (en) Liquid softener composition
EP0086104B1 (en) Method of softening fabrics
US5612309A (en) Nitrogen-free rinse cycle fabric softeners based on microemulsions
WO1997028244A1 (en) Process for making a fluid, stable liquid fabric softening composition including dispersible polyolefin
CA1192003A (en) Fabric softening composition
NZ260486A (en) Biodegradable fabric-softening compositions based on pentaerythritol esters and free of quaternary ammonium compounds
JPH09503009A (en) Rinse conditioner
MXPA01003077A (en) Fabric softening compositions containing pentaerythritol esters, bentonite and polyphosphonate

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19961213

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI NL PT SE

17Q First examination report despatched

Effective date: 19990614

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI NL PT SE

REF Corresponds to:

Ref document number: 206747

Country of ref document: AT

Date of ref document: 20011015

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 69523158

Country of ref document: DE

Date of ref document: 20011115

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: E. BLUM & CO. PATENTANWAELTE

ET Fr: translation filed
REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2165423

Country of ref document: ES

Kind code of ref document: T3

REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 20020103

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IE

Payment date: 20020424

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PT

Payment date: 20020524

Year of fee payment: 8

REG Reference to a national code

Ref country code: GR

Ref legal event code: EP

Ref document number: 20020400107

Country of ref document: GR

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20020613

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20020618

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20020717

Year of fee payment: 8

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20030513

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20030602

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20030603

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030609

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20030620

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030630

Ref country code: DK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030630

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030630

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030630

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 20030630

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20030808

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20030828

Year of fee payment: 9

BERE Be: lapsed

Owner name: *COLGATE-PALMOLIVE CY

Effective date: 20030630

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20031231

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

REG Reference to a national code

Ref country code: PT

Ref legal event code: MM4A

Free format text: LAPSE DUE TO NON-PAYMENT OF FEES

Effective date: 20031231

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GR

Payment date: 20040428

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040608

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040608

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040609

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040609

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050101

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050101

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20040608

EUG Se: european patent has lapsed
EUG Se: european patent has lapsed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050228

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20050101

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050608

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20040609

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20060103